HGVS | Genome Assembly |
---|---|
NC_000016.10:g.177404A>T , CM000678.2:g.177404A>T | GRCh38 |
NC_000016.9:g.227403A>T , CM000678.1:g.227403A>T | GRCh37 |
NC_000016.8:g.167403A>T | NCBI36 |
NG_000006.1:g.38267A>T | |
NG_059186.1:g.5754A>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000320868.9:c.422A>T MANE Select | ENSP00000322421.5:p.Tyr141Phe | |
ENST00000397797.1:c.326A>T | ENSP00000380899.1:p.Tyr109Phe | |
ENST00000472694.1:n.558A>T | ||
NM_000558.4:c.422A>T | NP_000549.1:p.Tyr141Phe | |
NM_000558.5:c.422A>T MANE Select | NP_000549.1:p.Tyr141Phe |